Evidence map›Paper›PMID 32371927›Full record

ArticleNature communications2020

Demographic and genetic factors influence the abundance of infiltrating immune cells in human tissues.

Andrew R Marderstein, Manik Uppal, Akanksha Verma, Bhavneet Bhinder, Zakieh Tayyebi, Jason Mezey, Andrew G Clark, Olivier Elemento

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
2.4field-weighted citation impact, top 10% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

30 citing papers in PubMed, 37 citations in OpenAlex.

  1. Article
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  7. An immunogenetic basis for lung cancer risk.Science (New York, N.Y.) · 2024
    Article
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  16. Review
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  18. Frontiers in medicine · 2022
    Article
  19. Review
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 1 institution in 2 countries.

Andrew R MardersteinTri-Institutional Program in Computational Biology & Medicine, Weill Cornell Medicine, New York, NY, USA.ORCID http://orcid.org/0000-0003-0859-4969
Manik UppalInstitute of Computational Biomedicine, Weill Cornell Medicine, New York, NY, USA.ORCID http://orcid.org/0000-0003-3628-1716
Akanksha VermaTri-Institutional Program in Computational Biology & Medicine, Weill Cornell Medicine, New York, NY, USA.
Bhavneet BhinderInstitute of Computational Biomedicine, Weill Cornell Medicine, New York, NY, USA.
Zakieh TayyebiTri-Institutional Program in Computational Biology & Medicine, Weill Cornell Medicine, New York, NY, USA.ORCID http://orcid.org/0000-0002-7821-9905
Jason MezeyTri-Institutional Program in Computational Biology & Medicine, Weill Cornell Medicine, New York, NY, USA.
Andrew G Clark *Tri-Institutional Program in Computational Biology & Medicine, Weill Cornell Medicine, New York, NY, USA. ac347@cornell.edu.ORCID http://orcid.org/0000-0001-7159-8511
Olivier Elemento *Tri-Institutional Program in Computational Biology & Medicine, Weill Cornell Medicine, New York, NY, USA. ole2001@med.cornell.edu.
Cornell University · US

Funding

Disparities in COVID Disease Severity and Outcomes in New York CityUL1TR002384 · NCATS · WEILL MEDICAL COLL OF CORNELL UNIV · PI JULIANNE L IMPERATO-MCGINLEY · 2017 to 2026
$86.2M
Tri-Institutional Training Program in Computational Biology & MedicineT32GM083937 · NIGMS · WEILL MEDICAL COLL OF CORNELL UNIV · PI CHRISTINI, DAVID J. · 2009 to 2018
$3.1M
The identification and validation of mechanisms and biomarkers for relapse in diffuse large B-cell lymphoma (Administrative Supplement)R01CA194547 · NCI · WEILL MEDICAL COLL OF CORNELL UNIV · PI ELEMENTO, OLIVIER, TAM, WAYNE · 2015 to 2019
$2.6M
NCATS NIH HHS UL1 TR002384NCI NIH HHS R01 CA194547NIGMS NIH HHS T32 GM083937
6 · The paper itself

Abstract

Despite infiltrating immune cells having an essential function in human disease and patients' responses to treatments, mechanisms influencing variability in infiltration patterns remain unclear. Here, using bulk RNA-seq data from 46 tissues in the Genotype-Tissue Expression project, we apply cell-type deconvolution algorithms to evaluate the immune landscape across the healthy human body. We discover that 49 of 189 infiltration-related phenotypes are associated with either age or sex (FDR < 0.1). Genetic analyses further show that 31 infiltration-related phenotypes have genome-wide significant associations (iQTLs) (P < 5.0 × 10

Indexed as

Polymorphism, Single NucleotideAdultAlgorithmsFemaleGene Expression ProfilingGene Regulatory NetworksGenetic Predisposition to DiseaseGenome-Wide Association StudyGenotypeHumansImmune SystemMaleMiddle AgedPhenotypeQuantitative Trait LociThyroid Gland

Identifiers

PMID32371927
PMCPMC7200670
OpenAlexW3023819387

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.